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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370668Generated: October 26, 2026

Hexane → 4-(2,2-Dibromovinyl)-4'-pentylbiphenyl

https://huagongshe.com/reaction/370668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant[1,1'-Biphenyl]-4-carboxaldehyde, 4'-pentyl-HCID 13250222—
SolventDichloromethaneHCID 6344—
Product4-(2,2-Dibromovinyl)-4'-pentylbiphenylHCID 2027495955%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 15.3 g of tetrabromomethane in 150 ml of methylene chloride was placed at 0° C. in a sulphonation flask under argon gasification and treated within 5 minutes with a solution of 12.1 g of triphenylphosphine in 50 ml of methylene chloride. After completion of the addition, the clear orange reaction solution was stirred at 0° C. for a further 5 minutes and then a solution of 5.80 g of 4-formyl-4'-pentylbiphenyl in 50 ml of methylene chloride was added dropwise within 10 minutes. After stirring at 0° C. for a further 45 minutes, the yellow-orange mixture was poured into 1000 ml of hexane and the precipitate which thereby separated was filtered off (rinsing with hexane). The concentrated filtrate was digested with 400 ml of hexane, left to stand at 0° C. for 18 hours, filtered (rinsing with hexane) and the filtrate was concentrated. Low-pressure chromatography (0.5 bar) of the residue (9.8 g) on silica gel with hexane gave 5.15 g (55%) of 4-(2,2-dibromovinyl)-4'-pentylbiphenyl as colourless crystals (purity 99.1%); m.p. 95° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528114
Source datasetuspto-grants-1985_07
ORD IDord-0f5f3bfb8f0f4b018277b9e2b4681e44
Source noteuspto-grants-1985_07